Skip to Content
Merck
  • NHC-catalyzed ring expansion of oxacycloalkane-2-carboxaldehydes: a versatile synthesis of lactones.

NHC-catalyzed ring expansion of oxacycloalkane-2-carboxaldehydes: a versatile synthesis of lactones.

Organic letters (2009-02-10)
Li Wang, Karen Thai, Michel Gravel
ABSTRACT

Imidazolinium-derived carbenes catalyze the ring-expansion lactonization of oxacycloalkane-2-carboxaldehydes. A variety of functionalized five-, six-, and seven-membered lactones can be formed efficiently under mild reaction conditions. The success of this new method for the construction of lactones is highly influenced by the electronic nature of the carbene catalyst.

MATERIALS
Product Number
Brand
Product Description

Sigma-Aldrich
1,3-Bis-(2,6-diisopropylphenyl)imidazolinium chloride, 97%